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[2,2'-Bipyridin]-3-amine, a member of the bipyridine family, is a chemical compound with the molecular formula C10H10N2. It features two pyridine rings and an amine group (-NH2) attached to the third position of the bipyridine ring, which endows the compound with unique properties. This versatile compound is widely used in coordination chemistry, materials science, organic synthesis, and medicinal chemistry due to its reactivity and ability to form stable complexes with various metal ions. It also holds potential for biological activities, making it a promising target for drug design and development.

105166-53-8

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105166-53-8 Usage

Uses

Used in Coordination Chemistry:
[2,2'-Bipyridin]-3-amine is used as a ligand for forming coordination complexes with metal ions. Its ability to chelate metal ions contributes to the stability and properties of the resulting complexes, making it a valuable component in the design of coordination compounds.
Used in Materials Science:
In the field of materials science, [2,2'-Bipyridin]-3-amine is utilized for its potential to create new materials with unique properties. Its capacity to form stable complexes with metal ions can lead to the development of materials with tailored characteristics for specific applications.
Used in Organic Synthesis:
[2,2'-Bipyridin]-3-amine serves as a building block in organic synthesis, where its reactivity and ability to form stable complexes can be exploited to synthesize a variety of organic compounds with different functionalities.
Used in Medicinal Chemistry:
In medicinal chemistry, [2,2'-Bipyridin]-3-amine is used as a starting material for the development of new drugs. Its potential biological activities and ability to form stable complexes with metal ions make it a promising candidate for the design of pharmaceutical agents.
Used in Drug Design and Development:
[2,2'-Bipyridin]-3-amine is considered for drug design and development due to its potential biological activities. Its unique structure and reactivity allow for the creation of compounds that can interact with biological targets, offering new therapeutic opportunities.

Check Digit Verification of cas no

The CAS Registry Mumber 105166-53-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,1,6 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105166-53:
(8*1)+(7*0)+(6*5)+(5*1)+(4*6)+(3*6)+(2*5)+(1*3)=98
98 % 10 = 8
So 105166-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H9N3/c11-8-4-3-7-13-10(8)9-5-1-2-6-12-9/h1-7H,11H2

105166-53-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyridin-2-ylpyridin-3-amine

1.2 Other means of identification

Product number -
Other names 3-amino-2,2'-bipyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:105166-53-8 SDS

105166-53-8Relevant academic research and scientific papers

Bipyridines. Part XVIII. On the Synthesis of -3-ol and Other Novel 2,2'-Bipyridine Derivatives from -3,3'-diamine

Kaczmarek, Lukasz

, p. 401 - 409 (2007/10/02)

-3-hydroxylamine (6) and its 3'-acetylderivative (7) were obtained by diazotization of -3,3'-diamine (3) in acetic acid, however, diazotization of copper(II) complex of 3 led to -3-amine (10).The amine 10 was transformed into -3-ol (2).The pethway of the reaction was proposed.

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